A citation-based method for searching scientific literature

Christoph Globas, Sophie Tezenas du Montcel, Laslo Baliko, Syliva Boesch, Chantal Depondt, Stefano DiDonato, Alexandra Durr, Alessandro Filla, Thomas Klockgether, Caterina Mariotti, Bela Melegh, Maryla Rakowicz, Pascale Ribai, Rafal Rola, Tanja Schmitz-Hubsch, Sandra Szymanski, Dagmar Timmann, Bart P Van de Warrenburg, Peter Bauer, Ludger Schols. Mov Disord 2008
Times Cited: 73







List of co-cited articles
755 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
917
42


Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Anna Sulek, Alexandra Durr, Perrine Charles,[...]. Lancet Neurol 2013
106
28

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
649
26

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles,[...]. Neurology 2008
167
24

Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.
Bart P C van de Warrenburg, Harrie Hendriks, Alexandra Dürr, Martin C A van Zuijlen, Giovanni Stevanin, Agnès Camuzat, Richard J Sinke, Alexis Brice, Berry P H Kremer. Ann Neurol 2005
79
23

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
A Dürr, G Stevanin, G Cancel, C Duyckaerts, N Abbas, O Didierjean, H Chneiweiss, A Benomar, O Lyon-Caen, J Julien,[...]. Ann Neurol 1996
334
20

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, Tanja Schmitz-Hübsch, Maryla Rakowicz, Caterina Mariotti, Ludger Schöls, Dagmar Timmann, Bart van de Warrenburg, Alexandra Dürr,[...]. Neuroimage 2010
109
17

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.
H Jacobi, P Bauer, P Giunti, R Labrum, M G Sweeney, P Charles, A Dürr, C Marelli, C Globas, C Linnemann,[...]. Neurology 2011
120
17

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael H Parkinson, Alexandra Durr, Alexis Brice, Perrine Charles,[...]. Lancet Neurol 2015
111
17

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
B P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, H Scheffer, E R Brunt, P F Ippel, J A Maat-Kievit, D Dooijes, N C Notermans, D Lindhout,[...]. Neurology 2002
159
16

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
16

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
15

Impaired eye movements in presymptomatic spinocerebellar ataxia type 6.
Peka Christova, John H Anderson, Christopher M Gomez. Arch Neurol 2008
29
34

The pathogenesis of spinocerebellar ataxia.
Arnulf H Koeppen. Cerebellum 2005
145
13

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Alfredo Brusco, Cinzia Gellera, Claudia Cagnoli, Alessandro Saluto, Alessia Castucci, Chiara Michielotto, Vincenza Fetoni, Caterina Mariotti, Nicola Migone, Stefano Di Donato,[...]. Arch Neurol 2004
100
12


Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings.
Heike Jacobi, Till-Karsten Hauser, Paola Giunti, Christoph Globas, Peter Bauer, Tanja Schmitz-Hübsch, László Baliko, Alessandro Filla, Caterina Mariotti, Maria Rakowicz,[...]. Cerebellum 2012
55
16

The wide spectrum of spinocerebellar ataxias (SCAs).
Mario-Ubaldo Manto. Cerebellum 2005
186
10

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
10

SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.
T Schmitz-Hübsch, P Giunti, D A Stephenson, C Globas, L Baliko, F Saccà, C Mariotti, M Rakowicz, S Szymanski, J Infante,[...]. Neurology 2008
79
10

Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1.
Janghoo Lim, Juan Crespo-Barreto, Paymaan Jafar-Nejad, Aaron B Bowman, Ronald Richman, David E Hill, Harry T Orr, Huda Y Zoghbi. Nature 2008
225
10

Oculomotor phenotypes in autosomal dominant ataxias.
N Buttner, D Geschwind, J C Jen, S Perlman, S M Pulst, R W Baloh. Arch Neurol 1998
97
10

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology.
P Trouillas, T Takayanagi, M Hallett, R D Currier, S H Subramony, K Wessel, A Bryer, H C Diener, S Massaquoi, C M Gomez,[...]. J Neurol Sci 1997
877
10

Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Jacqueline Medrano Montero, Gilberto Sánchez-Cruz, Raúl Aguilera-Rodríguez, Luis E Almaguer-Mederos, José M Laffita-Mesa. Lancet Neurol 2014
54
14

Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7.
Udo Rüb, Ludger Schöls, Henry Paulson, Georg Auburger, Pawel Kermer, Joanna C Jen, Kay Seidel, Horst-Werner Korf, Thomas Deller. Prog Neurobiol 2013
169
10

Brain pathology of spinocerebellar ataxias.
Kay Seidel, Sonny Siswanto, Ewout R P Brunt, Wilfred den Dunnen, Horst-Werner Korf, Udo Rüb. Acta Neuropathol 2012
208
10

The preclinical stage of spinocerebellar ataxias.
Roderick P P W M Maas, Judith van Gaalen, Thomas Klockgether, Bart P C van de Warrenburg. Neurology 2015
54
14

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Sophie Tezenas du Montcel, Alexandra Durr, Peter Bauer, Karla P Figueroa, Yaeko Ichikawa, Alessandro Brussino, Sylvie Forlani, Maria Rakowicz, Ludger Schöls, Caterina Mariotti,[...]. Brain 2014
93
10

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.
Sophie Tezenas du Montcel, Alexandra Durr, Maria Rakowicz, Lorenzo Nanetti, Perrine Charles, Anna Sulek, Caterina Mariotti, Rafal Rola, Ludger Schols, Peter Bauer,[...]. J Med Genet 2014
39
20

Toward understanding Machado-Joseph disease.
Maria do Carmo Costa, Henry L Paulson. Prog Neurobiol 2012
154
10

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.
Hiroki Takahashi, Kinya Ishikawa, Takeshi Tsutsumi, Hiroto Fujigasaki, Akihiro Kawata, Ryoichi Okiyama, Tsuneo Fujita, Kazuo Yoshizawa, Shigeki Yamaguchi, Hitoshi Tomiyasu,[...]. J Hum Genet 2004
48
14

Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.
Matthias Maschke, Gary Oehlert, Ting-Dong Xie, Susan Perlman, Sub H Subramony, Neeraj Kumar, Louis J Ptacek, Christopher M Gomez. Mov Disord 2005
37
18

Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
L Guerrini, F Lolli, A Ginestroni, G Belli, R Della Nave, C Tessa, S Foresti, M Cosottini, S Piacentini, F Salvi,[...]. Brain 2004
78
9

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, H Przuntek, J T Epplen, O Riess. Ann Neurol 1997
243
9

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.
I A Klement, P J Skinner, M D Kaytor, H Yi, S M Hersch, H B Clark, H Y Zoghbi, H T Orr. Cell 1998
797
9

Motor decline in clinically presymptomatic spinocerebellar ataxia type 2 gene carriers.
Luis Velázquez-Perez, Rosalinda Díaz, Ruth Pérez-González, Nalia Canales, Roberto Rodríguez-Labrada, Jacquelín Medrano, Gilberto Sánchez, Luis Almaguer-Mederos, Cira Torres, Juan Fernandez-Ruiz. PLoS One 2009
18
38

The natural history of degenerative ataxia: a retrospective study in 466 patients.
T Klockgether, R Lüdtke, B Kramer, M Abele, K Bürk, L Schöls, O Riess, F Laccone, S Boesch, I Lopes-Cendes,[...]. Brain 1998
223
9

Intensive coordinative training improves motor performance in degenerative cerebellar disease.
W Ilg, M Synofzik, D Brötz, S Burkard, M A Giese, L Schöls. Neurology 2009
141
9

Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument.
H Jacobi, M Rakowicz, R Rola, R Fancellu, C Mariotti, P Charles, A Dürr, M Küper, D Timmann, C Linnemann,[...]. Cerebellum 2013
58
12

Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment.
Sophie Tezenas du Montcel, Perrine Charles, Pascale Ribai, Cyril Goizet, Alice Le Bayon, Pierre Labauge, Lucie Guyant-Maréchal, Sylvie Forlani, Celine Jauffret, Nadia Vandenberghe,[...]. Brain 2008
55
12

Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.
Lynn Rochester, Brook Galna, Sue Lord, Dadirayi Mhiripiri, Gail Eglon, Patrick F Chinnery. Mov Disord 2014
24
29

Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2.
Luis Velázquez Pérez, Gilberto Sánchez Cruz, Nalia Canales Ochoa, Roberto Rodríguez Labrada, Julio Rodríguez Díaz, Luis Almaguer Mederos, José Laffita Mesa. J Neurol Sci 2007
35
17

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.
U Rüb, E R Brunt, E Petrasch-Parwez, L Schöls, D Theegarten, G Auburger, K Seidel, C Schultz, K Gierga, H Paulson,[...]. Neuropathol Appl Neurobiol 2006
58
10

Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
H Sasaki, H Kojima, I Yabe, K Tashiro, T Hamada, H Sawa, H Hiraga, K Nagashima. Acta Neuropathol 1998
71
8

CAG repeat disorder models and human neuropathology: similarities and differences.
Mitsunori Yamada, Toshiya Sato, Shoji Tsuji, Hitoshi Takahashi. Acta Neuropathol 2008
100
8

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families.
M L Moseley, K A Benzow, L J Schut, T D Bird, C M Gomez, P E Barkhaus, K A Blindauer, M Labuda, M Pandolfo, M D Koob,[...]. Neurology 1998
157
8



Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
J Vale, P Bugalho, I Silveira, J Sequeiros, J Guimarães, P Coutinho. Eur J Neurol 2010
41
14


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.